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Results: 1-25 | 26-49
Results: 1-25/49
PRESYMPTOMATIC TESTING FOR HEREDITARY BREAST OVARIAN CANCER (HBOC) - IS THERE PSYCHOLOGICAL DISTRESS IN THE PRETEST PERIOD/
Authors: LODDER LN FRETS PG TRIJSBURG RW DEWIT ACD TIBBEN A MEIJERSHEIJBOER EJ KLIJN JGM SEYNAEVE C NIERMEIJER MF
Citation: Ln. Lodder et al., PRESYMPTOMATIC TESTING FOR HEREDITARY BREAST OVARIAN CANCER (HBOC) - IS THERE PSYCHOLOGICAL DISTRESS IN THE PRETEST PERIOD/, European journal of cancer, 34, 1998, pp. 573-573
DISTRESS IN INDIVIDUALS FACING PREDICTIVE DNA TESTING FOR AUTOSOMAL-DOMINANT LATE-ONSET DISORDERS - COMPARING QUESTIONNAIRE RESULTS WITH IN-DEPTH INTERVIEWS
Authors: DUDOKDEWIT AC TIBBEN A DUIVENVOORDEN HJ NIERMEIJER MF PASSCHIER J TRIJSBURG RW LINDHOUT D MEIJERSHEIJBOER EJ FRETS PG FRETS PG LODDER LN ZOETEWIJ MW KLIJN JGM BROCKERVRIENDS A VANHAERINGEN A HELDERMAN ATJM HILHORSTHOFSTEE Y KANT S MAATKIEVIT JA OOSTERWIJK JC VANDERSMAGT JJ VEGTERVANDERVLIS M VRIESVANDERWEERD MACS ZOETEWEIJ MW BAKKER E DEVILEE P LOSEKOOT M TOPS C CORNELISSE CJ VASEN HFA
Citation: Ac. Dudokdewit et al., DISTRESS IN INDIVIDUALS FACING PREDICTIVE DNA TESTING FOR AUTOSOMAL-DOMINANT LATE-ONSET DISORDERS - COMPARING QUESTIONNAIRE RESULTS WITH IN-DEPTH INTERVIEWS, American journal of medical genetics, 75(1), 1998, pp. 62-74
COURSE OF DISTRESS EXPERIENCED BY PERSONS AT RISK FOR AN AUTOSOMAL-DOMINANT INHERITABLE DISORDER PARTICIPATING IN A PREDICTIVE TESTING PROGRAM - AN EXPLORATIVE STUDY
Authors: DEWIT ACD DUIVENVOORDEN HJ PASSCHIER J NIERMEIJER MF TIBBEN A
Citation: Acd. Dewit et al., COURSE OF DISTRESS EXPERIENCED BY PERSONS AT RISK FOR AN AUTOSOMAL-DOMINANT INHERITABLE DISORDER PARTICIPATING IN A PREDICTIVE TESTING PROGRAM - AN EXPLORATIVE STUDY, Psychosomatic medicine, 60(5), 1998, pp. 543-549
FAMILIAL AGGREGATION IN FRONTOTEMPORAL DEMENTIA
Authors: STEVENS M VANDUIJN CM KAMPHORST W DEKNIJFF P HEUTINK P VANGOOL WA SCHELTENS P RAVID R OOSTRA BA NIERMEIJER MF VANSWIETEN JC
Citation: M. Stevens et al., FAMILIAL AGGREGATION IN FRONTOTEMPORAL DEMENTIA, Neurology, 50(6), 1998, pp. 1541-1545
PREDICTING ADAPTATION TO PRESYMPTOMATIC DNA TESTING FOR LATE-ONSET DISORDERS - WHO WILL EXPERIENCE DISTRESS
Authors: DUDOKDEWIT AC TIBBEN A DUIVENVOORDEN HJ NIERMEIJER MF PASSCHIER J
Citation: Ac. Dudokdewit et al., PREDICTING ADAPTATION TO PRESYMPTOMATIC DNA TESTING FOR LATE-ONSET DISORDERS - WHO WILL EXPERIENCE DISTRESS, Journal of Medical Genetics, 35(9), 1998, pp. 745-754
MINOR DISEASE FEATURES IN NEUROFIBROMATOSIS TYPE-1 (NF1) AND THEIR POSSIBLE VALUE IN DIAGNOSIS OF NF1 IN CHILDREN LESS-THAN-OR-EQUAL-TO-6 YEARS AND CLINICALLY SUSPECTED OF HAVING NF1
Authors: CNOSSEN MH MOONS KGM GARSSEN MPJ PASMANS NMT DEGOEDEBOLDER A NIERMEIJER MF GROBBEE DE
Citation: Mh. Cnossen et al., MINOR DISEASE FEATURES IN NEUROFIBROMATOSIS TYPE-1 (NF1) AND THEIR POSSIBLE VALUE IN DIAGNOSIS OF NF1 IN CHILDREN LESS-THAN-OR-EQUAL-TO-6 YEARS AND CLINICALLY SUSPECTED OF HAVING NF1, Journal of Medical Genetics, 35(8), 1998, pp. 624-627
THE FRAGILE-X-SYNDROME
Authors: DEVRIES BBA HALLEY DJJ OOSTRA BA NIERMEIJER MF
Citation: Bba. Devries et al., THE FRAGILE-X-SYNDROME, Journal of Medical Genetics, 35(7), 1998, pp. 579-589
A PROSPECTIVE 10-YEAR FOLLOW-UP-STUDY OF PATIENTS WITH NEUROFIBROMATOSIS TYPE-1
Authors: CNOSSEN MH DEGOEDEBOLDER A VANDENBROEK KM WAASDORP CME ORANJE AP STROINK H SIMONSZ HJ VANDENOUWELAND AMW HALLEY DJJ NIERMEIJER MF
Citation: Mh. Cnossen et al., A PROSPECTIVE 10-YEAR FOLLOW-UP-STUDY OF PATIENTS WITH NEUROFIBROMATOSIS TYPE-1, Archives of Disease in Childhood, 78(5), 1998, pp. 408-412
DELETIONS SPANNING THE NEUROFIBROMATOSIS TYPE-1 GENE - IMPLICATIONS FOR GENOTYPE-PHENOTYPE CORRELATION IN NEUROFIBROMATOSIS TYPE-1
Authors: CNOSSEN MH VANDEREST MN BREUNING MH VANASPEREN CJ BRESLAUSIDERIUS EJ VANDERPLOEG AT DEGOEDEBOLDER A VANDENOUWELAND AMW HALLEY DJJ NIERMEIJER MF
Citation: Mh. Cnossen et al., DELETIONS SPANNING THE NEUROFIBROMATOSIS TYPE-1 GENE - IMPLICATIONS FOR GENOTYPE-PHENOTYPE CORRELATION IN NEUROFIBROMATOSIS TYPE-1, Human mutation, 9(5), 1997, pp. 458-464
HEREDITARY FRONTOTEMPORAL DEMENTIA IS LINKED TO CHROMOSOME-17Q21-Q22 - A GENETIC AND CLINICOPATHOLOGICAL STUDY OF 3 DUTCH FAMILIES
Authors: HEUTINK P STEVENS M RIZZU P BAKKER E KROS JM TIBBEN A NIERMEIJER MF VANDUIJN CM OOSTRA BA VANSWIETEN JC
Citation: P. Heutink et al., HEREDITARY FRONTOTEMPORAL DEMENTIA IS LINKED TO CHROMOSOME-17Q21-Q22 - A GENETIC AND CLINICOPATHOLOGICAL STUDY OF 3 DUTCH FAMILIES, Annals of neurology, 41(2), 1997, pp. 150-159
DIAGNOSTIC DELAY IN NEUROFIBROMATOSIS TYPE-1
Authors: CNOSSEN MH SMITH FJ DEGOEDEBOLDER A FRETS PG DUIVENVOORDEN HJ NIERMEIJER MF
Citation: Mh. Cnossen et al., DIAGNOSTIC DELAY IN NEUROFIBROMATOSIS TYPE-1, European journal of pediatrics, 156(6), 1997, pp. 482-487
INFORMING PARENTS ABOUT THE CARRIER STATUS OF THEIR FETUS
Authors: NIERMEIJER MF LOS FJ
Citation: Mf. Niermeijer et Fj. Los, INFORMING PARENTS ABOUT THE CARRIER STATUS OF THEIR FETUS, American journal of medical genetics, 73(4), 1997, pp. 489-489
FIRST-TRIMESTER DIAGNOSIS OF BLOMSTRAND LETHAL OSTEOCHONDRODYSPLASIA
Authors: DENHOLLANDER NS VANDERHARTEN HJ VERMEIJKEERS C NIERMEIJER MF WLADIMIROFF JW
Citation: Ns. Denhollander et al., FIRST-TRIMESTER DIAGNOSIS OF BLOMSTRAND LETHAL OSTEOCHONDRODYSPLASIA, American journal of medical genetics, 73(3), 1997, pp. 345-350
BRCA1 IN THE FAMILY - A CASE DESCRIPTION OF THE PSYCHOLOGICAL IMPLICATIONS
Authors: DUDOKDEWIT AC TIBBEN A FRETS PG MEIJERSHEIJBOER EJ DEVILEE P KLIJN JGM OOSTERWIJK JC NIERMEIJER MF
Citation: Ac. Dudokdewit et al., BRCA1 IN THE FAMILY - A CASE DESCRIPTION OF THE PSYCHOLOGICAL IMPLICATIONS, American journal of medical genetics, 71(1), 1997, pp. 63-71
GENETIC-COUNSELING BEFORE INTRACYTOPLASMIC SPERM INJECTION
Authors: VELD PAI HALLEY DJJ VANHEMEL JO NIERMEIJER MF DOHLE G WEBER RFA
Citation: Pai. Veld et al., GENETIC-COUNSELING BEFORE INTRACYTOPLASMIC SPERM INJECTION, Lancet, 350(9076), 1997, pp. 490-490
PSYCHOLOGICAL CONSEQUENCES OF PRESYMPTOMATIC TESTING FOR HUNTINGTONS-DISEASE
Authors: TIBBEN A ROOS RAC NIERMEIJER MF
Citation: A. Tibben et al., PSYCHOLOGICAL CONSEQUENCES OF PRESYMPTOMATIC TESTING FOR HUNTINGTONS-DISEASE, Lancet, 349(9054), 1997, pp. 809-809
PERINATAL NECROPSY BY MAGNETIC-RESONANCE-IMAGING
Authors: NIERMEIJER MF
Citation: Mf. Niermeijer, PERINATAL NECROPSY BY MAGNETIC-RESONANCE-IMAGING, Lancet, 349(9044), 1997, pp. 56-56
ENDOCRINOLOGIC DISORDERS AND OPTIC PATHWAY GLIOMAS IN CHILDREN WITH NEUROFIBROMATOSIS TYPE-1
Authors: CNOSSEN MH STAM EN COOIMAN LCMG SIMONSZ HJ STROINK H ORANJE AP HALLEY DJJ DEGOEDEBOLDER A NIERMEIJER MF KEIZERSCHRAMA SMPFD
Citation: Mh. Cnossen et al., ENDOCRINOLOGIC DISORDERS AND OPTIC PATHWAY GLIOMAS IN CHILDREN WITH NEUROFIBROMATOSIS TYPE-1, Pediatrics, 100(4), 1997, pp. 667-670
APOLIPOPROTEIN-E GENE AND SPORADIC FRONTAL-LOBE DEMENTIA
Authors: STEVENS M VANDUIJN CM DEKNIJFF P VANBROECKHOVEN C HEUTINK P OOSTRA BA NIERMEIJER MF VANSWIETEN JC
Citation: M. Stevens et al., APOLIPOPROTEIN-E GENE AND SPORADIC FRONTAL-LOBE DEMENTIA, Neurology, 48(6), 1997, pp. 1526-1529
PSYCHOLOGICAL DISTRESS IN APPLICANTS FOR PREDICTIVE DNA TESTING FOR AUTOSOMAL-DOMINANT, HERITABLE, LATE-ONSET DISORDERS
Authors: DUDOKDEWIT AC TIBBEN A DUIVENVOORDEN HJ FRETS PG ZOETEWEIJ MW LOSEKOOT M VANHAERINGEN A NIERMEIJER MF PASSCHIER J LINDHOUT D MEIJERSHEIJBOER EJ LODDER LN TRIJSBURG RW KLIJN JGM BROCKERVRIENDS A HELDERMAN ATJM HILHORSTHOFSTEE Y KANT S MAATKIEVIT JA OOSTERWIJK JC VANDERSMAGT JJ VEGTERVANDERVLIS M VRIESVANDERWEERD MACS BAKKER E CORNELISSE CJ DEVILEE P TOPS C VASEN HFA
Citation: Ac. Dudokdewit et al., PSYCHOLOGICAL DISTRESS IN APPLICANTS FOR PREDICTIVE DNA TESTING FOR AUTOSOMAL-DOMINANT, HERITABLE, LATE-ONSET DISORDERS, Journal of Medical Genetics, 34(5), 1997, pp. 382-390
DNA TESTING FOR FRAGILE-X-SYNDROME - IMPLICATIONS FOR PARENTS AND FAMILY
Authors: VANRIJN MA DEVRIES BBA TIBBEN A VANDENOUWELAND AMW HALLEY DJJ NIERMEIJER MF
Citation: Ma. Vanrijn et al., DNA TESTING FOR FRAGILE-X-SYNDROME - IMPLICATIONS FOR PARENTS AND FAMILY, Journal of Medical Genetics, 34(11), 1997, pp. 907-911
PREPARING FOR PRESYMPTOMATIC DNA TESTING FOR EARLY-ONSET ALZHEIMERS DISEASE CEREBRAL HEMORRHAGE AND HEREDITARY PICK DISEASE/
Authors: TIBBEN A STEVENS M DEWERT GMWR NIERMEIJER MF VANDUIJN CM VANSWIETEN JC
Citation: A. Tibben et al., PREPARING FOR PRESYMPTOMATIC DNA TESTING FOR EARLY-ONSET ALZHEIMERS DISEASE CEREBRAL HEMORRHAGE AND HEREDITARY PICK DISEASE/, Journal of Medical Genetics, 34(1), 1997, pp. 63-72
A FRAGILE-X SCREENING-PROGRAM IN THE NETHERLANDS - PREVALENCE OF FRAGILE-X-SYNDROME LOWER THAN PREVIOUSLY CONSIDERED, BUT THE DISORDER IS STILL UNDERDIAGNOSED
Authors: DEVRIES BBA VANDENOUWELAND AMW MOHKAMSING S DUIVENVOORDEN HJ HALLEY DJJ SANDKUIJL LA OOSTRA BA TIBBEN A NIERMEIJER MF
Citation: Bba. Devries et al., A FRAGILE-X SCREENING-PROGRAM IN THE NETHERLANDS - PREVALENCE OF FRAGILE-X-SYNDROME LOWER THAN PREVIOUSLY CONSIDERED, BUT THE DISORDER IS STILL UNDERDIAGNOSED, American journal of human genetics, 61(4), 1997, pp. 1267-1267
SCREENING AND DIAGNOSIS FOR THE FRAGILE-X-SYNDROME AMONG THE MENTALLY-RETARDED - AN EPIDEMIOLOGIC AND PSYCHOLOGICAL SURVEY
Authors: DEVRIES BBA VANDENOUWELAND AMW MOHKAMSING S DUIVENVOORDEN HJ MOL E GELSEMA K VANRIJN M HALLEY DJJ SANDKUIJL LA OOSTRA BA TIBBEN A NIERMEIJER MF
Citation: Bba. Devries et al., SCREENING AND DIAGNOSIS FOR THE FRAGILE-X-SYNDROME AMONG THE MENTALLY-RETARDED - AN EPIDEMIOLOGIC AND PSYCHOLOGICAL SURVEY, American journal of human genetics, 61(3), 1997, pp. 660-667
GERM-LINE AND SOMATIC MOSAICISM IN THE ANDROGEN INSENSITIVITY SYNDROME - IMPLICATIONS FOR GENETIC-COUNSELING
Authors: BOEHMER ALM BRINKMANN AO NIERMEIJER MF BAKKER L HALLEY DJJ DROP SLS
Citation: Alm. Boehmer et al., GERM-LINE AND SOMATIC MOSAICISM IN THE ANDROGEN INSENSITIVITY SYNDROME - IMPLICATIONS FOR GENETIC-COUNSELING, American journal of human genetics, 60(4), 1997, pp. 1003-1006
Risultati: 1-25 | 26-49